Canonical Allele Identifier: CA16043660
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 374300
ClinVar RCV Id: RCV000415251
dbSNP Id: rs1057518682

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127420174del , CM000667.2:g.127420174del GRCh38
NC_000005.9:g.126755866del , CM000667.1:g.126755866del GRCh37
NC_000005.8:g.126783765del NCBI36
NG_032072.1:g.134411del
NG_032072.2:g.134411del

Transcript Alleles

HGVS Amino-acid change
ENST00000503335.7:c.1557del MANE Select ENSP00000423354.2:p.Trp520GlyfsTer17
ENST00000274473.6:c.1557del ENSP00000274473.6:p.Trp520GlyfsTer17
ENST00000418761.6:c.1557del ENSP00000416284.2:p.Trp520GlyfsTer17
ENST00000503335.6:c.1557del ENSP00000423354.2:p.Trp520GlyfsTer17
ENST00000508365.5:c.1557del ENSP00000423195.1:p.Trp520GlyfsTer17
NM_001256545.1:c.1557del NP_001243474.1:p.Trp520GlyfsTer17
NM_001308119.1:c.1557del NP_001295048.1:p.Trp520GlyfsTer17
NM_001308121.1:c.1557del NP_001295050.1:p.Trp520GlyfsTer17
NM_032446.2:c.1557del NP_115822.1:p.Trp520GlyfsTer17
XM_011543692.1:c.1557del XP_011541994.1:p.Trp520GlyfsTer17
XM_011543693.1:c.1557del XP_011541995.1:p.Trp520GlyfsTer17
XM_011543694.1:c.1557del XP_011541996.1:p.Trp520GlyfsTer17
XM_017009987.1:c.1722del XP_016865476.1:p.Trp575GlyfsTer17
XM_017009988.1:c.417del XP_016865477.1:p.Trp140GlyfsTer17
NM_001256545.2:c.1557del MANE Select NP_001243474.1:p.Trp520GlyfsTer17
NM_032446.3:c.1557del NP_115822.1:p.Trp520GlyfsTer17
NM_001308119.2:c.1557del NP_001295048.1:p.Trp520GlyfsTer17
NM_001308121.2:c.1557del NP_001295050.1:p.Trp520GlyfsTer17